Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates

Detalhes bibliográficos
Autor(a) principal: Viana-Niero, C. [UNIFESP]
Data de Publicação: 2004
Outros Autores: Haas, P. E. de, van Soolingen, D., Leao, S. C. [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/27681
http://dx.doi.org/10.1099/mic.0.26778-0
Resumo: The Mycobacterium tuberculosis genome contains four highly related genes which present significant similarity to Pseudomonas aeruginosa genes encoding phospholipase C enzymes. Three of these genes, plcA, plcB and plcC, are organized in tandem (locus pIcABC). the fourth gene, plcD, is located in a different region. This study investigates variations in plcABC and plcD genes in clinical isolates of M. tuberculosis, Mycobacterium africanum and 'Mycobacterium canettii'. Genetic polymorphisms were examined by PCR, Southern blot hybridization, sequence analysis and RT-PCR. Seven M. tuberculosis isolates contain insertions of IS61 10 elements within plcA, plcC or plcD. in 19 of 25 M. tuberculosis isolates examined, genomic deletions were identified, resulting in loss of parts of genes or complete genes from the plcABC and/or plcD loci. Partial plcD deletion was observed in one M. africanum isolate. in each case, deletions were associated with the presence of a copy of the IS61 10 element and in all occurrences IS61 10 was transposed in the same orientation. A mechanism of deletion resulting from homologous recombination of two copies of IS61 10 was recognized in a group of genetically related M. tuberculosis isolates. Five M. tuberculosis isolates presented major polymorphisms in the plcABC and plcD regions, along with loss of expression competence that affected all four plc genes. Phospholipase C is a well-known bacterial virulence factor. the precise role of phospholipase C in the pathogenicity of M. tuberculosis is unknown, but considering the potential importance that the plc genes may have in the virulence of the tubercle bacillus, the study of isolates cultured from patients with active tuberculosis bearing genetic variations affecting these genes may provide insights into the significance of phospholipase C enzymes for tuberculosis pathogenicity.
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spelling Viana-Niero, C. [UNIFESP]Haas, P. E. devan Soolingen, D.Leao, S. C. [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Natl Inst Publ Hlth & Environm2016-01-24T12:37:04Z2016-01-24T12:37:04Z2004-04-01Microbiology-sgm. Reading: Soc General Microbiology, v. 150, p. 967-978, 2004.1350-0872http://repositorio.unifesp.br/handle/11600/27681http://dx.doi.org/10.1099/mic.0.26778-010.1099/mic.0.26778-0WOS:000221067000023The Mycobacterium tuberculosis genome contains four highly related genes which present significant similarity to Pseudomonas aeruginosa genes encoding phospholipase C enzymes. Three of these genes, plcA, plcB and plcC, are organized in tandem (locus pIcABC). the fourth gene, plcD, is located in a different region. This study investigates variations in plcABC and plcD genes in clinical isolates of M. tuberculosis, Mycobacterium africanum and 'Mycobacterium canettii'. Genetic polymorphisms were examined by PCR, Southern blot hybridization, sequence analysis and RT-PCR. Seven M. tuberculosis isolates contain insertions of IS61 10 elements within plcA, plcC or plcD. in 19 of 25 M. tuberculosis isolates examined, genomic deletions were identified, resulting in loss of parts of genes or complete genes from the plcABC and/or plcD loci. Partial plcD deletion was observed in one M. africanum isolate. in each case, deletions were associated with the presence of a copy of the IS61 10 element and in all occurrences IS61 10 was transposed in the same orientation. A mechanism of deletion resulting from homologous recombination of two copies of IS61 10 was recognized in a group of genetically related M. tuberculosis isolates. Five M. tuberculosis isolates presented major polymorphisms in the plcABC and plcD regions, along with loss of expression competence that affected all four plc genes. Phospholipase C is a well-known bacterial virulence factor. the precise role of phospholipase C in the pathogenicity of M. tuberculosis is unknown, but considering the potential importance that the plc genes may have in the virulence of the tubercle bacillus, the study of isolates cultured from patients with active tuberculosis bearing genetic variations affecting these genes may provide insights into the significance of phospholipase C enzymes for tuberculosis pathogenicity.Universidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, EPM, BR-04023062 São Paulo, BrazilNatl Inst Publ Hlth & Environm, Diagnost Lab Infect Dis & Perinatal Screening, NL-3720 BA Bilthoven, NetherlandsUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, EPM, BR-04023062 São Paulo, BrazilWeb of Science967-978engSoc General MicrobiologyMicrobiology-sgmAnalysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolatesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/276812022-06-02 09:02:18.52metadata only accessoai:repositorio.unifesp.br:11600/27681Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:13:36.574584Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates
title Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates
spellingShingle Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates
Viana-Niero, C. [UNIFESP]
title_short Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates
title_full Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates
title_fullStr Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates
title_full_unstemmed Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates
title_sort Analysis of genetic polymorphisms affecting the four phospholipase C (plc) genes in Mycobacterium tuberculosis complex clinical isolates
author Viana-Niero, C. [UNIFESP]
author_facet Viana-Niero, C. [UNIFESP]
Haas, P. E. de
van Soolingen, D.
Leao, S. C. [UNIFESP]
author_role author
author2 Haas, P. E. de
van Soolingen, D.
Leao, S. C. [UNIFESP]
author2_role author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Natl Inst Publ Hlth & Environm
dc.contributor.author.fl_str_mv Viana-Niero, C. [UNIFESP]
Haas, P. E. de
van Soolingen, D.
Leao, S. C. [UNIFESP]
description The Mycobacterium tuberculosis genome contains four highly related genes which present significant similarity to Pseudomonas aeruginosa genes encoding phospholipase C enzymes. Three of these genes, plcA, plcB and plcC, are organized in tandem (locus pIcABC). the fourth gene, plcD, is located in a different region. This study investigates variations in plcABC and plcD genes in clinical isolates of M. tuberculosis, Mycobacterium africanum and 'Mycobacterium canettii'. Genetic polymorphisms were examined by PCR, Southern blot hybridization, sequence analysis and RT-PCR. Seven M. tuberculosis isolates contain insertions of IS61 10 elements within plcA, plcC or plcD. in 19 of 25 M. tuberculosis isolates examined, genomic deletions were identified, resulting in loss of parts of genes or complete genes from the plcABC and/or plcD loci. Partial plcD deletion was observed in one M. africanum isolate. in each case, deletions were associated with the presence of a copy of the IS61 10 element and in all occurrences IS61 10 was transposed in the same orientation. A mechanism of deletion resulting from homologous recombination of two copies of IS61 10 was recognized in a group of genetically related M. tuberculosis isolates. Five M. tuberculosis isolates presented major polymorphisms in the plcABC and plcD regions, along with loss of expression competence that affected all four plc genes. Phospholipase C is a well-known bacterial virulence factor. the precise role of phospholipase C in the pathogenicity of M. tuberculosis is unknown, but considering the potential importance that the plc genes may have in the virulence of the tubercle bacillus, the study of isolates cultured from patients with active tuberculosis bearing genetic variations affecting these genes may provide insights into the significance of phospholipase C enzymes for tuberculosis pathogenicity.
publishDate 2004
dc.date.issued.fl_str_mv 2004-04-01
dc.date.accessioned.fl_str_mv 2016-01-24T12:37:04Z
dc.date.available.fl_str_mv 2016-01-24T12:37:04Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Microbiology-sgm. Reading: Soc General Microbiology, v. 150, p. 967-978, 2004.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/27681
http://dx.doi.org/10.1099/mic.0.26778-0
dc.identifier.issn.none.fl_str_mv 1350-0872
dc.identifier.doi.none.fl_str_mv 10.1099/mic.0.26778-0
dc.identifier.wos.none.fl_str_mv WOS:000221067000023
identifier_str_mv Microbiology-sgm. Reading: Soc General Microbiology, v. 150, p. 967-978, 2004.
1350-0872
10.1099/mic.0.26778-0
WOS:000221067000023
url http://repositorio.unifesp.br/handle/11600/27681
http://dx.doi.org/10.1099/mic.0.26778-0
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Microbiology-sgm
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 967-978
dc.publisher.none.fl_str_mv Soc General Microbiology
publisher.none.fl_str_mv Soc General Microbiology
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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